Optimizing the antibacterial activity of a lead structure discovered by ‘SAR by MS’ technology-Reference-Cited by-同舟云学术

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Optimizing the antibacterial activity of a lead structure discovered by ‘SAR by MS’ technology

Published:2004-11 Issue:21 Volume:14 Page:5257-5261
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Jefferson Elizabeth A.,Seth Punit P.,Robinson Dale E.,Winter Dana K.,Miyaji Alycia,Risen Lisa M.,Osgood Stephen A.,Bertrand Myra,Swayze Eric E.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference18 articles.

1. Can better prescribing turn the tide of resistance?

2. Why is big Pharma getting out of antibacterial drug discovery?

3. RNA-targeted therapeutics: prospects and promise

4. Targeting RNA: new opportunities to address drugless targets

5. Emerging Developments in RNA Therapeutics

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1. Fragment-Based Approaches to Identify RNA Binders;Journal of Medicinal Chemistry;2023-05-15

2. Recent Advances in Synthesis and Uses of Heterocycles-based Palladium(II) Complexes as Robust, Stable, and Low-cost Catalysts for Suzuki- Miyaura Crosscouplings;Current Organic Chemistry;2019-10-28

3. Synthesis of biaryl-linked cyclic peptoids;Tetrahedron Letters;2017-03

4. Fragment-Based Drug Design: Strategic Advances and Lessons Learned;Comprehensive Medicinal Chemistry III;2017

5. Pd(II)-Catalyzed Bidentate Directing Group-Aided Chemoselective Acetoxylation of Remote ε-C(sp2)–H Bonds in Heteroaryl–Aryl-Based Biaryl Systems;The Journal of Organic Chemistry;2016-12-07

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